A Longitudinal Study on Family Adaptation and Relationship Dynamics in Pediatric Rare Diseases

Rare Diseases

rare diseases, family adaptation, family functioning, psychological adjustment, psychosocial adjustment, quality of life, longitudinal study, caregiver experience, ecological momentary assessment, children and adolescents

Rare diseases in children can affect not only the child's health but also the well-being and relationships within the entire family. Parents often experience stress, uncertainty, and emotional strain, which may in turn influence their child's mental health and quality of life. However, little is known about how families adapt over time to living with a rare disease or how daily experiences and family interactions shape this process. This study aims to better understand how children with rare diseases and their caregivers adjust psychologically and emotionally over time. It will examine how factors such as parental stress, uncertainty, coping strategies, and family communication are linked to the mental health and quality of life of both children and parents. The study will include children and adolescents (ages 1-18) with a diagnosed rare disease and their caregivers. Participants will complete online questionnaires at four time points over one year. A subgroup of families will also take part in a two-week smartphone-based assessment, where parents report their daily experiences, such as stress, emotions, and worries, several times per day. Some children and adolescents will additionally participate in interviews to share their own perspectives. The main outcomes of interest are the child's mental health and quality of life. The study will also assess parental well-being and family functioning to understand how these factors influence each other over time. By combining long-term and daily data, this study will provide a detailed picture of how families cope with rare diseases in everyday life. The findings may help improve psychological support and guide the development of targeted interventions for families affected by rare pediatric conditions.

Rare diseases (RDs) are chronic conditions that often begin in childhood and can have lifelong consequences for affected individuals and their families. In addition to physical health challenges, families frequently face significant psychological and social burdens, including stress, uncertainty about the future, and disruptions in daily life. While prior research has mainly focused on medical aspects of rare diseases, less is known about how families adapt over time and how interactions between children and their caregivers influence psychological outcomes. This study is based on a theoretical model of family adaptation that integrates individual, relational, and contextual factors. In particular, it focuses on cognitive and emotional processes such as intolerance of uncertainty, illness perceptions, and coping strategies, as well as family-level processes including communication, parenting, and shared experiences of illness ("we-disease"). The study adopts a systemic perspective, recognizing that the well-being of children and caregivers is interdependent and evolves over time. The project uses a longitudinal design with four assessment waves over a 12-month period, complemented by annual follow-ups. This design allows for the investigation of both stability and change in psychological adjustment. Data will be collected using standardized, validated questionnaires assessing mental health, health-related quality of life, stress, and family functioning. To better capture the child's perspective, a subset of children and adolescents will participate in structured interviews at each time point. In addition to the longitudinal component, a subgroup of families will participate in an Ecological Sampling Method (ESM) phase. During this two-week period, caregivers will report multiple times per day on their current emotional state, stress levels, worries, perceived uncertainty, and coping responses using a smartphone application. This intensive data collection approach enables the examination of short-term, real-life dynamics and within-person fluctuations that cannot be captured through traditional survey methods. The study will apply advanced statistical methods to analyze both longitudinal and intensive repeated-measures data. Actor-Partner Interdependence Models (APIM) and related approaches will be used to examine reciprocal relationships between child and caregiver outcomes over time, while multilevel modeling will be used to analyze daily processes captured in the ESM phase. By integrating these approaches, the study aims to identify both long-term adaptation patterns and short-term mechanisms that contribute to psychological adjustment. The overall goal of the project is to generate a comprehensive understanding of how families adapt to pediatric rare diseases, including identifying risk and protective factors at the individual and family level. The findings are expected to inform the development of targeted psychosocial interventions, improve clinical support for affected families, and contribute to a more holistic approach to rare disease care that addresses both medical and psychosocial needs.

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